
PTSM: Pharmaceutical Technology Sourcing and Management
- PTSM: Pharmaceutical Technology Sourcing and Management-02-03-2016
- Volume 12
- Issue 2
Aesica Pharmaceuticals Relocates Services to Queenborough
Aesica Pharmaceuticals, a global pharmaceutical contract development and manufacturing organization (CDMO), announced the strategic relocation of development and clinical manufacturing services from Nottingham to Queenborough. The new development center at Queenborough has more than twice the capacity of the existing one in Nottingham.
Aesica Pharmaceuticals, a global pharmaceutical contract development and manufacturing organization (CDMO), announced the strategic relocation of development and clinical manufacturing services from Nottingham to Queenborough. The new development center at Queenborough has more than twice the capacity of the existing one in Nottingham.
According to a Jan. 19, 2016 press announcement from the company, Aesica will now provide full manufacturing and development services at its Queenborough site with the addition of a new development center. From Queenborough, the company now provides API production, formulation development, and clinical manufacture through to commercial-scale product manufacturing.
The new development center will be able to handle potent and controlled drugs, which mirror the commercial offering from Queenborough. The company will also still offer semi-solid development and inhalation services.
Source:
Articles in this issue
almost 10 years ago
Is Consolidation Good for Pharma?almost 10 years ago
Parenteral Packagers Focus on Security and Supply-Chain Transparencyalmost 10 years ago
Nanoparticles Demonstrate Potential for Small-Molecule Pharmaceuticalsalmost 10 years ago
Hermes Pharma Adds Hot Melt Coating Capabilityalmost 10 years ago
Novasep Adds Small-Scale Manufacturing Capability to US Facilityalmost 10 years ago
Vetter Completes Development and IT Facilityalmost 10 years ago
Adents, Siemens Team on Serialization Solutionalmost 10 years ago
Onyx Scientific Announces Facility Expansionalmost 10 years ago
GS1 US Expands Advisory Services Program to Address Industry Challengesalmost 10 years ago
FDA’s CDER Previews 2016 Guidance AgendaNewsletter
Get the essential updates shaping the future of pharma manufacturing and compliance—subscribe today to Pharmaceutical Technology and never miss a breakthrough.





